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Entinostat

Product Specifications

Product Name Alternative

MS-275; SNDX-275

UNSPSC Description

Entinostat is an oral and selective class I HDAC inhibitor, with IC50s of 243 nM, 453 nM, and 248 nM for HDAC1, HDAC2, and HDAC3, respectively.

Target Antigen

Apoptosis; Autophagy; HDAC

Type

Reference compound

Related Pathways

Apoptosis;Autophagy;Cell Cycle/DNA Damage;Epigenetics

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/Entinostat.html

Purity

99.82

Solubility

DMSO : 50 mg/mL (ultrasonic;warming;heat to 60°C)

Smiles

O=C(NCC1=CC=C(C=C1)C(NC2=CC=CC=C2N)=O)OCC3=CC=CN=C3

Molecular Weight

376.41

References & Citations

[1]Lauffer BE, et al. Histone deacetylase (HDAC) inhibitor kinetic rate constants correlate with cellular histone acetylation but not transcription and cell viability. J Biol Chem. 2013 Sep 13;288(37):26926-43.|[2]Rosato RR, et al. The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1 1. Cancer Res. 2003 Jul 1;63(13):36|[3]Saito A, et al. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc Natl Acad Sci U S A, 1999, 96(8), 4592-4597.|[4]Zhang ZY, et al. MS-275, an histone deacetylase inhibitor, reduces the inflammatory reaction in rat experimental autoimmune neuritis. Neurosci, 2010, 169, 370-377.

Shipping Conditions

Blue Ice

Storage Conditions

-20°C, 3 years (Powder)

Product Datasheet

http://file.medchemexpress.com/batch_PDF/HY-12163/Entinostat-DataSheet-MedChemExpress.pdf

Product MSDS

http://file.medchemexpress.com/batch_PDF/HY-12163/Entinostat-SDS-MedChemExpress.pdf

Clinical Information

Phase 3

CAS Number

209783-80-2

Available Sizes

Curated Selection

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